A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041452



Internal ID19130671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928314..18940429hg38UCSC Ensembl
Innerchr11:18949861..18961976hg19UCSC Ensembl
Innerchr11:18906437..18918552hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812116
hg1912116
hg1812116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3511963
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041452
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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